Effect of Li2CO3 additive on gas generation in lithium-ion batteries

被引:203
作者
Shin, JS
Han, CH
Jung, UH
Lee, SI
Kim, HJ
Kim, K [1 ]
机构
[1] Korea Univ, Div Chem & Mol Engn, Dept Chem, Seoul 136701, South Korea
[2] Korea Univ, Dept Chem Engn, Seoul 136701, South Korea
[3] LG Chem Ltd, Battery Res Ctr, Taejon 305380, South Korea
关键词
Li-ion batteries; additives; gas generation; SEI; Li2CO3;
D O I
10.1016/S0378-7753(02)00039-3
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
To elucidate the mechanism of gas generation during charge-discharge cycling of a lithium-ion cell, the generated gases and passive films on the carbon electrode are examined by means of gas chromatography (GC) and Fourier transform infrared (FTIR) spectroscopy. In ethyl carbonate/dimethyl carbonate and ethyl carbonate/diethyl carbonate 1 M LiPF6 electrolytes, the detected gaseous products are CO2, CO, CH4, C2H4, C2H6, etc. The FTIR spectrum of the surface of the carbon electrode shows bands which correspond to Li2CO3, ROCO2Li, (ROCO2Li)(2), and RCO2Li. These results suggest that gas evolution is caused by electrode decomposition, reactive trace impurities, and electrolyte reduction. The surface of the electrode is composed of electrolyte reduction products. When 0.05 M Li2CO3 is added as an electrolyte additive, the total volume of generated gases is reduced, and the discharge capacity and the conductivity of lithium-ions are increased. These results can be explained by a more compact and thin 'solid electrolyte interface' film on the carbon electrode formed by Li2CO3, which effectively prevents solvent co-intercalation and carbon exfoliation. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
相关论文
共 29 条
[11]   THE DEPENDENCE OF THE PERFORMANCE OF LI-C INTERCALATION ANODES FOR LI-ION SECONDARY BATTERIES ON THE ELECTROLYTE SOLUTION COMPOSITION [J].
EINELI, Y ;
MARKOVSKY, B ;
AURBACH, D ;
CARMELI, Y ;
YAMIN, H ;
LUSKI, S .
ELECTROCHIMICA ACTA, 1994, 39 (17) :2559-2569
[12]   THE CORRELATION BETWEEN THE CYCLING EFFICIENCY, SURFACE-CHEMISTRY AND MORPHOLOGY OF LI ELECTRODES IN ELECTROLYTE-SOLUTIONS BASED ON METHYL FORMATE [J].
EINELI, Y ;
AURBACH, D .
JOURNAL OF POWER SOURCES, 1995, 54 (02) :281-288
[13]   The role of SO2 as an additive to organic Li-ion battery electrolytes [J].
EinEli, Y ;
Thomas, SR ;
Koch, VR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (04) :1159-1165
[14]   STUDIES OF LITHIUM INTERCALATION INTO CARBONS USING NONAQUEOUS ELECTROCHEMICAL-CELLS [J].
FONG, R ;
VONSACKEN, U ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (07) :2009-2013
[15]   Impedance study on the electrochemical lithium intercalation into natural graphite powder [J].
Funabiki, A ;
Inaba, M ;
Ogumi, Z ;
Yuasa, S ;
Otsuji, J ;
Tasaka, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (01) :172-178
[16]   Gas generation mechanism due to electrolyte decomposition in commercial lithium-ion cell [J].
Kumai, K ;
Miyashiro, H ;
Kobayashi, Y ;
Takei, K ;
Ishikawa, R .
JOURNAL OF POWER SOURCES, 1999, 81 :715-719
[17]   Simultaneous measurements and modeling of the electrochemical impedance and the cyclic voltammetric characteristics of graphite electrodes doped with lithium [J].
Levi, MD ;
Aurbach, D .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (23) :4630-4640
[18]   Thermal stability studies of Li-ion cells and components [J].
Maleki, H ;
Deng, GP ;
Anani, A ;
Howard, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (09) :3224-3229
[19]   MECHANISM LEADING TO IRREVERSIBLE CAPACITY LOSS IN LI ION RECHARGEABLE BATTERIES [J].
MATSUMURA, Y ;
WANG, S ;
MONDORI, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (09) :2914-2918
[20]   Fluoroethylene carbonate electrolyte and its use in lithium ion batteries with graphite anodes [J].
McMillan, R ;
Slegr, H ;
Shu, ZX ;
Wang, WD .
JOURNAL OF POWER SOURCES, 1999, 81 :20-26